HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630375Generated: October 27, 2026
Sodium hydride → HCID 178486063, compound
https://huagongshe.com/reaction/630375
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl alpha-hydroxy-alpha-2-thienyl-2-thiopheneacetate | HCID 11414137 | — |
| Reactant | HCID 178486055 | HCID 178486055 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178486063 | HCID 178486063 | 69% |
Reaction Steps
To a solution of methyl hydroxy(di-2-thienyl)acetate (5.8 g, 0.02 mol) (prepared according to Acta Chemica Scandinavica 24 (1970) 1590-1596) in anhydrous toluene (95 mL) was first added a solution of tert-butyl (trans-4-hydroxycyclohexyl)-methylcarbamate (intermediate 3; 6 g, 0.02 mol) in anhydrous toluene (95 mL) and secondly sodium hydride (60%, 0.45 g, 0.01 mol). After few minutes the mixture was warmed to 155° C. and the solvent was distilled and simultaneously replaced. This procedure was carried on during 1 hour and a half. The mixture was cooled to room temperature and diluted with ether (300 mL). The organic layer was washed with sodium bicarbonate 4% (2×200 mL) and brine, dried, filtered and evaporated over reduced pressure giving the title compound as a yellow solid (69%), which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315463B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-7436c803cbbe452885049419e4e00181 |
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| Source note | uspto-grants-2016_04 |
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